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510(k) K890381

Device
PARAMETRIUM CLAMP
Applicant
KINETIC MEDICAL PRODUCTS
510(k) number
K890381
Product code
HXD  
Decision
Substantially Equivalent (SESE)
Decision date
1989-02-03
Date received
1989-01-23
Regulation
878.4800
Classification name
Clamp
Medical specialty
General & Plastic Surgery
Review panel
General & Plastic Surgery
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
JAMES I LAUGHNER
Address
4934 Peach St. Erie PA US 16509 16509

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code HXD  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K890368KIDNEY CLAMPKinetic Medical Products1989-02-03
K890371INTESTINAL CRUSHING CLAMPKinetic Medical Products1989-02-03
K890372INTESTINAL CLAMPKinetic Medical Products1989-02-03
K874959VASCULAR CLAMPSolway, Inc.1987-12-30
K872386C CLAMPMed-Tool, Inc.1987-07-02
K863653SUCTION-OFFB&B Medical Technologies, Inc.1986-10-07
K853538CANNULA CLAMPCp Medical1985-09-12
K851654OMNIMED CLAMPOmni Intl., Inc.1985-05-31
K801819SURGICAL INSTRUMENTSRobert I. Chien & Assoc., Inc.1980-08-20
K801028RICA OR SMIC SURGICAL INSTRUMENTSRobert I. Chien & Assoc., Inc.1980-05-20
K791289GIZMO TOWEL CLAMPHemoy, Inc.1979-07-24
K782090CLAMP, DISPOSABLEConcord Laboratories, Inc.1978-12-20
K770118CARPENTER BONE CLAMPStryker Corp.1977-01-26

Legacy Summary#

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FDA Review#

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